Rho is hiring a Biostatistician II for our Federal Research Team. This job includes communicating statistical issues as they arise to Rho team members as well as maintaining a steady, open dialogue with study team members regarding study execution as it relates to timelines, data quality, and interpretation of the results. Rho's environment is team-oriented. Good communication skills and the ability to work with a team are crucial for success. Rho's high quality standards require careful attention to accuracy and details.
Develop, test, maintain, and archive SAS program code to conduct planned and exploratory statistical analysis of clinical data
Interpret the results using written, oral, and graphic methods, as appropriate, either in a statistical report or as part of a clinical trial report
Develop CDISC compliant datasets
Prepare analysis plans and specifications for analysis data sets and data displays (tables, listings, & graphs)
Collaborate with statistical programming team on the production of datasets and displays
Identify and troubleshoot missing, miscoded, or incomplete data and work with clinical team to resolve issues
Perform sample size computations in conjunction with clinical staff to determine the appropriate number of subjects necessary for the investigation, taking into consideration the interpretability of the results from a statistical and clinical perspective as well as applicable regulatory requirements
Develop and/or validate randomization schemes for clinical trials
Manage project responsibilities with decreasing levels of supervision or regular support
Takes initiative to complete project-specific responsibilities with minimal supervision
Master's degree in (bio)statistics and 2 years of experience working in a CRO or a doctoral degree in (bio)statistics and no relevant experience, or an equivalent combination of relevant education and/or work experience.
Good understanding of basic statistical procedures and methodology is required along with strong SAS programming skills
Excellent organizational skills, written and verbal communication skills, and working knowledge of Microsoft Office Suite is a must
Ability to work on several projects simultaneously and manage deadlines
Familiarity with CDISC standards is a strong plus
Rho is a full-service contract research organization optimally sized to deliver results from clinical research with agility and adaptability. Maximizing profitability, stability, and planned growth has helped provide us with the experience, capacities, and capabilities of a larger organization—all without losing touch with our entrepreneurial passion.
Because Rho recognizes great people are our most important asset, we attract and retain the best and brightest.
Changing what it means to work with a CRO.
At Rho, we believe expertise is everything. With a demonstrated track record of success, we guide our clients through the most appropriate program strategies, navigate the unique challenges of clinical trials, and drive development of the high-quality marketing applications demanded by regulatory authorities.
Our experts take clients beyond procedural operations and into truly proactive problem-solving. Through a collaborative approach and individualized attention, our focus is advancing your program so that together, we can help heal the world.
That is what drives us.